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Tricellulin Antikörper

MARVELD2 Reaktivität: Human, Ratte, Maus WB, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7264717
  • Target Alle Tricellulin (MARVELD2) Antikörper anzeigen
    Tricellulin (MARVELD2)
    Reaktivität
    • 32
    • 11
    • 10
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Ratte, Maus
    Wirt
    • 32
    Kaninchen
    Klonalität
    • 32
    Polyklonal
    Konjugat
    • 15
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser Tricellulin Antikörper ist unkonjugiert
    Applikation
    • 24
    • 15
    • 14
    • 3
    • 2
    • 2
    Western Blotting (WB), Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    A synthetic peptide of human MARVELD2 (NP_001033692.2).
    Isotyp
    IgG
  • Applikationshinweise
    WB 1:500-1:2000 IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Tricellulin (MARVELD2)
    Andere Bezeichnung
    MARVELD2 (MARVELD2 Produkte)
    Synonyme
    Mrvldc2 antikoerper, BC003296 antikoerper, MARVD2 antikoerper, Tric antikoerper, Trica antikoerper, Tricb antikoerper, Tricc antikoerper, DFNB49 antikoerper, MRVLDC2 antikoerper, MARVEL domain containing 2 antikoerper, MARVEL (membrane-associating) domain containing 2 antikoerper, Marveld2 antikoerper, MARVELD2 antikoerper
    Hintergrund
    The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene.
    Molekulargewicht

    Observed_MW: 64 kDa

    Calculated_MW: 51 kDa/62 kDa/64 kDa

    Gen-ID
    153562
    UniProt
    Q8N4S9
    Pathways
    Sensory Perception of Sound, Cell-Cell Junction Organization
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